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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5976071copy number variation1nstd209human GRCh38 chrX: 134,381,381-134,387,880 , GRCh37.p13 chrX: 133,515,411-133,521,910 PHF6
    nsv5975977copy number variation1nstd209human GRCh38 chrX: 134,423,843-134,429,592 , GRCh37.p13 chrX: 133,557,873-133,563,622 PHF6
    nsv5881941copy number variation1nstd209human GRCh38 chrX: 134,373,466-134,377,569 , GRCh37.p13 chrX: 133,507,496-133,511,599 PHF6
    nsv5881355copy number variation1nstd209human GRCh38 chrX: 134,384,902-134,386,666 , GRCh37.p13 chrX: 133,518,932-133,520,696 PHF6
    nsv5881137copy number variation1nstd209human GRCh38 chrX: 134,393,635-134,413,487 , GRCh37.p13 chrX: 133,527,665-133,547,517 PHF6
    nsv5879503copy number variation1nstd209human GRCh38 chrX: 134,396,794-134,397,830 , GRCh37.p13 chrX: 133,530,824-133,531,860 PHF6
    nsv5877552copy number variation1nstd209human GRCh38 chrX: 134,413,657-134,413,821 , GRCh37.p13 chrX: 133,547,687-133,547,851 PHF6
    nsv5877285copy number variation1nstd209human GRCh38 chrX: 134,425,328-134,425,657 , GRCh37.p13 chrX: 133,559,358-133,559,687 PHF6
    nsv5876258copy number variation1nstd209human GRCh38 chrX: 134,377,754-134,378,002 , GRCh37.p13 chrX: 133,511,784-133,512,032 PHF6
    nsv5874191copy number variation1nstd209human GRCh38 chrX: 134,378,105-134,393,498 , GRCh37.p13 chrX: 133,512,135-133,527,528 PHF6
    nsv5871755copy number variation1nstd209human GRCh38 chrX: 134,413,965-134,415,013 , GRCh37.p13 chrX: 133,547,995-133,549,043 PHF6
    nsv5871432copy number variation1nstd209human GRCh38 chrX: 134,384,705-134,809,218 , GRCh37.p13 chrX: 133,518,735-133,943,248 MIR503, MIR450A1, 15 more genes
    nsv5870967copy number variation1nstd209human GRCh38 chrX: 134,386,897-134,389,033 , GRCh37.p13 chrX: 133,520,927-133,523,063 PHF6
    nsv5673904copy number variation1nstd102humanPathogenic GRCh37 chrX: 132,670,132-133,634,127 , GRCh38.p12 chrX: 133,536,104-134,500,097 TIMM8BP2, MIR106A, 14 more genes
    nsv5420497copy number variation1nstd206human GRCh38 chrX: 134,384,862-134,386,744 , GRCh37.p13 chrX: 133,518,892-133,520,774 PHF6
    nsv5418669copy number variation1nstd206human GRCh38 chrX: 134,412,257-134,412,491 , GRCh37.p13 chrX: 133,546,287-133,546,521 PHF6
    nsv5416490copy number variation1nstd206human GRCh38 chrX: 134,423,576-134,424,957 , GRCh37.p13 chrX: 133,557,606-133,558,987 PHF6
    nsv5414344copy number variation1nstd206human GRCh38 chrX: 134,386,900-134,389,034 , GRCh37.p13 chrX: 133,520,930-133,523,064 PHF6
    nsv5377093translocation1nstd200human GRCh38 chrX: 134,386,900-134,386,900 , GRCh38 chrX: 134,389,034-134,389,034 , GRCh37.p13 chrX: 133,520,930-133,520,930 , GRCh37.p13 chrX: 133,523,064-133,523,064 PHF6
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